The following data is part of a premarket notification filed by Ivoclar North America, Inc. with the FDA for D-sign Vi (r&d Project Dw266#9).
| Device ID | K990235 |
| 510k Number | K990235 |
| Device Name: | D-SIGN VI (R&D PROJECT DW266#9) |
| Classification | Alloy, Metal, Base |
| Applicant | IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | Peter P Mancuso |
| Correspondent | Peter P Mancuso IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
| Product Code | EJH |
| CFR Regulation Number | 872.3710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-01-25 |
| Decision Date | 1999-03-01 |